Canonical Allele Identifier: CA2576094629
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88835218del , CM000678.2:g.88835218del GRCh38
NC_000016.9:g.88901626del , CM000678.1:g.88901626del GRCh37
NC_000016.8:g.87429127del NCBI36
NG_008667.1:g.26750del

Transcript Alleles

HGVS Amino-acid Change
ENST00000268695.10:c.894del MANE Select ENSP00000268695.5:p.Glu298AspfsTer21
ENST00000268695.9:c.894del ENSP00000268695.5:p.Glu298AspfsTer21
ENST00000562593.5:n.4303del
ENST00000562931.5:n.482del
ENST00000567525.5:c.575del ENSP00000454484.1:n.575del
ENST00000568613.5:c.1013del ENSP00000457921.1:n.1013del
NM_000512.4:c.894del NP_000503.1:p.Glu298AspfsTer21
XM_005256301.2:c.894del XP_005256358.1:p.Glu298AspfsTer21
XM_005256302.1:c.912del XP_005256359.1:p.Glu304AspfsTer21
XM_011522982.1:c.912del XP_011521284.1:p.Glu304AspfsTer21
XM_011522984.1:c.912del XP_011521286.1:p.Glu304AspfsTer21
NM_001323543.1:c.339del NP_001310472.1:p.Glu113AspfsTer21
NM_001323544.1:c.912del NP_001310473.1:p.Glu304AspfsTer21
XM_005256301.3:c.894del XP_005256358.1:p.Glu298AspfsTer21
XM_011522982.2:c.912del XP_011521284.1:p.Glu304AspfsTer21
XM_017023111.2:c.912del XP_016878600.1:p.Glu304AspfsTer21
XM_017023112.2:c.912del XP_016878601.1:p.Glu304AspfsTer21
XM_017023113.1:c.339del XP_016878602.1:p.Glu113AspfsTer21
NM_000512.5:c.894del MANE Select NP_000503.1:p.Glu298AspfsTer21
NM_001323543.2:c.339del NP_001310472.1:p.Glu113AspfsTer21
NM_001323544.2:c.912del NP_001310473.1:p.Glu304AspfsTer21